Canonical Allele Identifier: CA2766252871

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706701G>T , CM000686.2:g.19706701G>T	GRCh38
NC_000024.9:g.21868587G>T , CM000686.1:g.21868587G>T	GRCh37
NC_000024.8:g.20327975G>T	NCBI36
NG_032920.1:g.43239C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4070-61C>A MANE Select	ENSP00000322408.4:n.4070-61C>A
ENST00000317961.8:c.4070-61C>A	ENSP00000322408.4:n.4070-61C>A
ENST00000382806.6:c.3899-61C>A	ENSP00000372256.2:n.3899-61C>A
ENST00000440077.5:c.3947-61C>A	ENSP00000398543.1:n.3947-61C>A
ENST00000469599.6:n.2760C>A
ENST00000492117.1:n.4054C>A
ENST00000541639.5:c.4163-61C>A	ENSP00000444293.1:n.4163-61C>A
NM_001146705.1:c.4163-61C>A	NP_001140177.1:n.4163-61C>A
NM_001146706.1:c.3899-61C>A	NP_001140178.1:n.3899-61C>A
NM_004653.4:c.4070-61C>A	NP_004644.2:n.4070-61C>A
XM_005262560.1:c.3935-61C>A	XP_005262617.1:n.3935-61C>A
XM_005262561.1:c.3839-61C>A	XP_005262618.1:n.3839-61C>A
XM_011531468.1:c.3992-61C>A	XP_011529770.1:n.3992-61C>A
XR_244571.2:n.4358-93C>A
XR_430568.2:n.4784C>A
XM_005262560.3:c.3935-61C>A	XP_005262617.1:n.3935-61C>A
XM_005262561.3:c.3839-61C>A	XP_005262618.1:n.3839-61C>A
XM_011531468.3:c.3992-61C>A	XP_011529770.1:n.3992-61C>A
XM_024452495.1:c.2060-61C>A	XP_024308263.1:n.2060-61C>A
XM_024452496.1:c.1826-61C>A	XP_024308264.1:n.1826-61C>A
XR_001756009.2:n.4808-61C>A
XR_001756010.2:n.4808-93C>A
XR_001756011.2:n.4673-61C>A
XR_001756012.2:n.4821-61C>A
XR_001756013.2:n.4139-61C>A
XR_002958832.1:n.4332C>A
XR_002958834.1:n.4464-61C>A
XR_002958835.1:n.4347-61C>A
XR_002958836.1:n.5030-93C>A
XR_002958837.1:n.4837-93C>A
XR_244571.4:n.4357-93C>A
XR_430568.4:n.4783C>A
NM_001146706.2:c.3899-61C>A	NP_001140178.1:n.3899-61C>A
NM_004653.5:c.4070-61C>A MANE Select	NP_004644.2:n.4070-61C>A
NM_001146705.2:c.4163-61C>A	NP_001140177.1:n.4163-61C>A